Home NDC 63868-704 Anti Nausea Liquid
Product NDC 63868-704
11-digit product format 638680704
Labeler code 63868
Product ID 63868-704_451d7339-57de-f89c-e063-6394a90a09e1
Type HUMAN OTC DRUG
Nonproprietary name dextrose(glucose),Levulose(fructose),Phosphoric acid
Dosage form SOLUTION
Route ORAL
Labeler QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2019-04-16
Substance DEXTROSE, UNSPECIFIED FORM; FRUCTOSE; PHOSPHORIC ACID
Active strength 1.87; 1.87; 21.5 g/5mL; g/5mL; mg/5mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Anti Nausea Liquid
Brand name suffix Cherry Flavor
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DEXTROSE, UNSPECIFIED FORM 1.87 g/5mL FRUCTOSE 1.87 g/5mL PHOSPHORIC ACID 21.5 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination IY9XDZ35W2 Internal UNII lookup 6YSS42VSEV Internal UNII lookup E4GA8884NN Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 318146 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63868-704-04 Anti Nausea LiquidCherry Flavor 1 in 1 CARTON SOLUTION 1 6 63868-704-04 Anti Nausea LiquidCherry Flavor 118 mL in 1 BOTTLE SOLUTION 118 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63868-704 ANTI NAUSEA LIQUID CHERRY FLAVOR (DEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACID) SOLUTION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)] 5 Current NDC, Legacy NDC, 2 package rows 20241222_743b215a-81cc-408c-9375-4f427161a05b.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63868-704-04 63868070404 1 BOTTLE in 1 CARTON (63868-704-04) / 118 mL in 1 BOTTLE 1 bottle 2019-04-16 0000-00-00 No No Current